Marucco Arianna, Prono Marion, Beal David, Alasonati Enrica, Fisicaro Paola, Bergamaschi Enrico, Carriere Marie, Fenoglio Ivana
Department of Chemistry, University of Torino, 10125 Torino, Italy.
Chimie Interface Biologie pour l'Environnement, la Santé et la Toxicologie (CIBEST), University Grenoble Alpes, CEA, CNRS, IRIG, SyMMES, F-38000 Grenoble, France.
Nanomaterials (Basel). 2020 Oct 27;10(11):2132. doi: 10.3390/nano10112132.
Oral exposure to titanium dioxide (TiO) is common since it is widely used in food and pharmaceutical products. Concern on the safety of this substance has been recently raised, due to the presence of an ultrafine fraction in food-grade TiO. Discrepancy exists among data reported in in vitro and in vivo studies on intestinal acute/chronic toxicity of TiO. This might be due to the different biological identity of TiO in traditional in vitro test by respect in vivo conditions. One food-grade TiO and two nanometric TiO samples were treated with a simulated human digestive dystem (SHDS) in order to investigate the bio-transformation occurring to the particles once ingested in term of size distribution (Dynamic Light Scattering-DLS-, Flow Particle Imaging, Asymmetric Flow Field Flow Fractionation-AF4-) and surface modification (Electrophoretic Light Scattering-ELS-, Electron Paramagnetic Resonance Spectroscopy-EPR-). The effect of SHDS on the cyto-, genotoxicity and potential to induce oxidative stress towards human colorectal carcinoma HCT116 cells was also assessed. Aggregation as a consequence of the high ionic strength of the gastric and intestinal simulated fluids was observed, together with the formation of a partially irreversible bio-corona containing phosphate ions and proteins. Such bio-corona led to a partial masking of the TiO particles surface and reactivity. Pristine and treated TiO nanoparticles showed comparable acute toxicity and genotoxicity toward HCT116 cells, whereas a small decrease of the induction of oxidative stress after treatment was observed. Overall the results underline the importance of SHDS as a tool to improve the predictive power of in vitro tests towards intestinal nanomaterial toxicity.
由于二氧化钛(TiO₂)广泛应用于食品和药品中,经口接触该物质很常见。近期,由于食品级TiO₂中存在超细颗粒,人们对该物质的安全性产生了担忧。关于TiO₂肠道急/慢性毒性的体外和体内研究报告的数据存在差异。这可能是由于传统体外试验中TiO₂的生物学特性与体内条件不同所致。为了研究摄入后颗粒在尺寸分布(动态光散射-DLS-、流动颗粒成像、不对称流场流分级-AF4-)和表面修饰(电泳光散射-ELS-、电子顺磁共振光谱-EPR-)方面发生的生物转化,对一种食品级TiO₂和两种纳米级TiO₂样品进行了模拟人体消化系统(SHDS)处理。还评估了SHDS对人结肠直肠癌HCT116细胞的细胞毒性、遗传毒性以及诱导氧化应激的潜力。观察到由于胃和肠道模拟液的高离子强度导致颗粒聚集,同时形成了含有磷酸根离子和蛋白质的部分不可逆的生物冠。这种生物冠导致TiO₂颗粒表面和反应性部分被掩盖。原始和处理后的TiO₂纳米颗粒对HCT116细胞表现出相当的急性毒性和遗传毒性,而处理后氧化应激诱导略有下降。总体而言,结果强调了SHDS作为一种提高体外试验对肠道纳米材料毒性预测能力的工具的重要性。